When man tries to imagine Paradise For the purposes of this experiment we will ignore the effects of ion
on earth, the immediate result is interaction. In fact, we will be using a very soluble salt, KNO3, because it has
a very respectable Hell.
--Paul Claudel
The Thermodynamics of Solubility Equilibrium
In addition to the homogeneous equilibrium you have investigated in earlier
experiments, an important heterogeneous equilibrium exists for many salts and their
solutions. At some point as solute concentration is increased the solubility limit at a
given temperature is reached. We say the solution is "saturated". Typically some
undissolved solute will remain in the mixture and thus the potential for equilibrium
between the solid phase and the dissolved solute in solution exists. For a hypothetical
salt A2B, the solubility equilibrium and equilibrium constant are expressed as:
A2B(s) ' 2 A+(aq) + B2-(aq)
+ 2 2-
Kc = [A ] [B ]
The amount of A2B that dissolves is the "solubility" which can be expressed in any
convenient units--here moles/Litre or Molarity is useful. From the reaction above you
can see that this amount is the same as the amount of B2- ion that enters the solution.
Thus if we use the letter s to represent the solubility of A2B, we can rewrite the
equilibrium constant as:
Kc = (2s)2s
Notice that the quantity 2s is substituted for [A+]. This maintains the stoichiometric
relationship with [B2-] while allowing the use of a single variable. Because the
equilibrium constant is expressed as the product (as in multiplication) of solubilities, it
is generally called the "solubility product constant" and given the symbol Ksp.
Typically when we speak about Ksp values we are interested in very slightly
soluble salts--the kinds of compounds you learned as "insoluble" in your solubility
rules. But the quantity can be calculated for any salt as long as you have solubility data.
However, determining Ksp values from simple experiments in which solubility is
measured almost never yields accurate results, even for very insoluble compounds.
The reasons for this are complex and have to do with ion interactions which occur in all
but the most dilute of solutions. In other words, there are "ideal" solutions (the kind we
talk about) and "real" solutions (the kind we steer clear of) just as there are ideal and
real gases.
Adapted from: Solubility and Thermodynamics: An Introductory Experiment, Robert
G. Silbereman, J. Chem. Educ., 1996, vol. 73, No. 5, p. 426
characteristics that make it easy to work with, it's inexpensive, relatively harmless as
used, and easily recovered for reuse.
The equilibrium established in a saturated solution of KNO3 may be
represented as:
KNO3(s) ' K+(aq) + NO3-(aq)
As with all equilibria, the relative amounts of products and reactants at a given
temperature are determined by the "tension" between the tendency toward maximum
entropy and the tendency toward minimum energy. In this experiment you will first
determine the solubility of potassium nitrate at a variety of temperatures and then use
the solubility to calculate the "Ksp" of the salt. Recall the relationship between the
equilibrium constant and the free energy change, ∆Go:
∆Go = -RTlnK
where R = 8.31 J/mol·K and T is the temperature in Kelvin. So you can determine the
free energy change at each temperature from the Ksp at each temperature.
The sign of the enthalpy change (∆H) should be clear from the solubility
behavior (i.e., whether more or less dissolves at higher temperatures) but the value of
∆H can also be determined from the value of the Ksp. It is known that over small
temperature ranges, K and ∆H are related as follows:
∆H 1
ln K = - +C
R T
y = m x + b
So a plot of the natural logs of the values of Ksp vs. 1/T (in Kelvin) will yield a nearly
straight line with slope = -∆H/R (again, R = 8.31 J/mol·K).
And, of course, once you know ∆G and ∆H, you can determine ∆S at each
temperature. Again, it should be clear what the sign of the entropy change will be
considering the process.
To summarize: you will determine the solubility of KNO3 in water at different
temperatures and use this information to calculate the "Ksp" of the salt. From the Ksp
you will determine the free energy change, enthalpy change and entropy change for this
process and compare them to the values calculated from tables in your text.
Preparing to experiment
You will be provided with the following materials:
1. solid KNO3 (use about 3 g)
2. a temperature probe
3. a boiling water bath
Design an experiment to determine the temperature at which KNO3 becomes insoluble
in water (to start, add distilled water to the 4 mL mark with the solid already in the
cylinder), gradually diluting the solution by 3 additions of 1 mL each and repeating the
measurements. [see Technique]
BE SURE TO BRING YOUR TI-83/P CALCULATOR TO
CLASS FOR THIS EXPERIMENT. YOU WILL ALSO
NEED A COPY OF THE HCHEM.83G FILES IN YOUR
CALCULATOR MEMORY.
Pre-lab take-home quiz
These questions should be answered on a separate sheet of paper to be turned in on the
day you do this experiment.
1. The solubility of ZnS at 25 oC is 3.5 x 10-12 M. What is the Ksp for ZnS? What is ∆G?
2. The Ksp for Ag2S is 4.1 x 10-52. What is [Ag+] in a saturated solution of Ag2S?
3. The Ksp for Ag2CrO4 is 9.0 x 10-12. Calculate the Ag+ concentration necessary to just
start precipitation in a 0.00025 M CrO42- solution.
Technique
1. Determining the solubility
In order to determine the solubility in moles/Litre you need to know the moles
of solute (easy) and the volume of the solution. To make this second piece of
information easier to get, you can do the experiment in your 10 mL graduated cylinder
(remove the plastic base before heating). The initial volume can be read directly from
the cylinder once the solid has dissolved (stir in the hot water). Each 1 mL addition
thereafter will increase the volume, but again you should record the volume only after
redissolving the solid in the hot water bath.
Try to minimize the amount of time the cylinder spends in the hot water, i.e.,
don't leave it there any longer than needed to dissolve the solid. Otherwise you will
spend a lot of time waiting for the solution to cool before crystals form. Always keep
the solution stirred and record the first temperature that crystals become visible.
Experience seems to indicate that the falling temperature levels off a little as
crystallization occurs. Be careful not to lose solid as you remove the thermometer probe
from the cylinder to add more water.
KEEP THE THERMOMETER PROBE CABLE AWAY FROM THE
HOTPLATE!!!!!!!!
2. Recycling the KNO3
After you have your four readings, pour your solution into the beaker indicated
by your instructor. The water can be evaporated and the potassium nitrate reused.
The Chemicals
Potassium nitrate is commonly known as "saltpeter". It is a colorless, odorless solid
with a saline, pungent taste. It is used in fireworks, pickling brines, the manufacture of
glass, matches, gunpowder, freezing mixtures and candle wicks.
Analysis
1. Use the mass of KNO3 and the measured volumes of the various mixtures to
calculate the Molarities (solubilities) for each of the four trials.
2. Plot a graph of the solubility of KNO3 (in mole/L) vs. the temperature. What does
this graph suggest about the sign of ∆H for this process? Explain.
3. Use the calculated solubilities to determine the "Ksp" for potassium nitrate at the four
temperatures measured. Then plot a graph as described in the introduction to determine
the value of ∆H for this process. The ∆Hfo values for the process are given below.
KNO3(s) ' K+(aq) + NO3-(aq)
-492.7 -251.2 -206.6 kJ/mol
Calculate ∆Hrxn from them. Explain any disagreement.
4. Calculate the free energy change for this process at each of the four temperatures
measured, using your "Ksp" values from #3. The ∆Gfo values for the process are given
below:
KNO3(s) ' K+(aq) + NO3-(aq)
-393.1 -282.3 -110.6 kJ/mol
Calculate ∆Grxn from them. Explain any disagreement.
5. Use the experimental values of ∆G and ∆H to calculate ∆S at each of the four
temperatures. The So values for the process are given below:
KNO3(s) ' K+(aq) + NO3-(aq)
+132.9 +102.5 +146.4 J/mol·K
Calculate ∆Srxn from them. Explain any disagreement. How does the sign on ∆S "fit"
this process? Is this process entropy or enthalpy driven--or both? Explain.
Now the "truth"
You already know that we choose to assume gases behave ideally because it greatly
simplifies ordinary work in the lab and some of the mathematics that goes along with it.
The same is true about solutions. What you have learned about the equilibrium in
saturated solutions is true enough, but what you have not been told is that ions, even in
rather dilute solutions, can clump together in groups, or establish quite large hydration
spheres with water, etc. In other words, sometimes the actual concentration of "ions" in
a solution is difficult to determine by simple experimental means.
The most accurate determinations of Ksp are done by examining successively more
dilute solutions in light of a mathematical model of "real" solutions. When this is done
and the ion concentration is extrapolated to zero, the "official" Ksp or what is sometimes
call the thermodynamic Ksp is found. This value should come close to the value you
would get if you found ∆Go for the process and then used the expression ∆Go = -
RTlnKsp to determine the Ksp. This often results in disagreements between ordinary
experimental values and calculated values related by factors of 10 or 100!!!!
MORAL: Basic solubility and Ksp concepts are deceptively simple and not meant to be
strictly mathematical.